Canonical Allele Identifier: CA2807473150

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810117_68810118del , CM000678.2:g.68810117_68810118del	GRCh38
NC_000016.9:g.68844020_68844021del , CM000678.1:g.68844020_68844021del	GRCh37
NC_000016.8:g.67401521_67401522del	NCBI36
NG_008021.1:g.77826_77827del , LRG_301:g.77826_77827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.688-80_688-79del MANE Select	ENSP00000261769.4:n.688-80_688-79del
ENST00000261769.9:c.688-80_688-79del	ENSP00000261769.4:n.688-80_688-79del
ENST00000422392.6:c.688-80_688-79del	ENSP00000414946.2:n.688-80_688-79del
ENST00000561751.1:c.454+1269_454+1270del
ENST00000562836.5:n.759-80_759-79del
ENST00000566510.5:c.532-80_532-79del	ENSP00000458139.1:n.532-80_532-79del
ENST00000566612.5:c.688-80_688-79del	ENSP00000454782.1:n.688-80_688-79del
ENST00000611625.4:c.688-80_688-79del	ENSP00000481063.1:n.688-80_688-79del
ENST00000612417.4:c.688-80_688-79del	ENSP00000478360.1:n.688-80_688-79del
ENST00000621016.4:c.688-80_688-79del	ENSP00000480664.1:n.688-80_688-79del
NM_004360.3:c.688-80_688-79del , LRG_301t1:c.688-80_688-79del	NP_004351.1:n.688-80_688-79del
XM_011523488.1:c.-48-80_-48-79del	XP_011521790.1:n.-48-80_-48-79del
XM_011523489.1:c.-48-80_-48-79del	XP_011521791.1:n.-48-80_-48-79del
NM_001317184.1:c.688-80_688-79del	NP_001304113.1:n.688-80_688-79del
NM_001317185.1:c.-928-80_-928-79del	NP_001304114.1:n.-928-80_-928-79del
NM_001317186.1:c.-1132-80_-1132-79del	NP_001304115.1:n.-1132-80_-1132-79del
NM_004360.4:c.688-80_688-79del	NP_004351.1:n.688-80_688-79del
NM_004360.5:c.688-80_688-79del MANE Select	NP_004351.1:n.688-80_688-79del
NM_001317184.2:c.688-80_688-79del	NP_001304113.1:n.688-80_688-79del
NM_001317185.2:c.-928-80_-928-79del	NP_001304114.1:n.-928-80_-928-79del
NM_001317186.2:c.-1132-80_-1132-79del	NP_001304115.1:n.-1132-80_-1132-79del